On-line solid-phase extraction of large-volume injections coupled to liquid chromatography-tandem mass spectrometry for the quantitation and confirmation of 14 selected trace organic contaminants in drinking and surface water

被引:99
作者
Garcia-Ac, Araceli [1 ]
Segura, Pedro A. [1 ]
Viglino, Liza [1 ]
Furtos, Alexandra [1 ]
Gagnon, Christian [2 ]
Prevost, Michele [3 ]
Sauve, Sebastien [1 ]
机构
[1] Univ Montreal, Dept Chem, Montreal, PQ H3C 3J7, Canada
[2] Environm Canada, Sci & Technol Branch, Montreal, PQ H2Y 2E7, Canada
[3] Ecole Polytech, Montreal, PQ H3C 3A7, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
On-line solid-phase extraction; LC-MS/MS; LC-TOFMS; Emerging contaminants; Pesticides; Pharmaceuticals and personal care products; Surface water; Drinking water; PERSONAL-CARE PRODUCTS; ANTI-INFECTIVES; LEVEL DETERMINATION; PHARMACEUTICALS; PESTICIDES; ELECTROSPRAY; SORBENTS; PRECONCENTRATION; QUANTIFICATION; IDENTIFICATION;
D O I
10.1016/j.chroma.2009.10.015
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We describe the development and validation of an on-line solid-phase extraction of large-volume injections coupled to liquid chromatography-tandem mass spectrometry method for the simultaneous quantitation and confirmation of 14 selected trace organic contaminants in drinking and surface water. Selected compounds were: anti-infectives (clarithromycin, sulfamethoxazole and trimethoprim), an anticonvulsant (carbamazepine) and its transformation product 10,11-dihydrocarbamazepine, an antihypertensive (enalapril), antineoplastics (cyclophosphamide and methotrexate), herbicides (atrazine, cyanazine. and simazine) and two of their transformation products (deethylatrazine and deisopropylatrazine) and an antiseptic (triclocarban). The breakthrough volume determinations showed that out of all the investigated sorbents, the Strata-X on-line solid-phase extraction column showed the best performance. The method used a load volume of 10.0 mL and was validated using the corresponding matrices, yielding for most compounds, R-2 > 0.99. Extraction recoveries ranged from 60 to 109%. The intra- and inter-day precision were <14 and <16%, respectively. The method detection limits ranged from 0.6 to 6 ng L-1. Matrix effects were in general low. The performance of the on-line method was demonstrated with the analysis of real water samples. The application of alternative techniques of confirmation was also explored using accurate mass measurements on a time-of-flight mass spectrometer and the data-dependent reverse energy ramp scan on a triple quadrupole. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:8518 / 8527
页数:10
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